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Ale intervertebral fusion device system - Taiwan Registration 5bc96fbdd9efd89bc5a0727cb234b260

Access comprehensive regulatory information for Ale intervertebral fusion device system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5bc96fbdd9efd89bc5a0727cb234b260 and manufactured by JBone Biotechnology Co.,Ltd.. The authorized representative in Taiwan is JBone Biotechnology Co.,Ltd..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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5bc96fbdd9efd89bc5a0727cb234b260
Registration Details
Taiwan FDA Registration: 5bc96fbdd9efd89bc5a0727cb234b260
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Device Details

Ale intervertebral fusion device system
TW: ไบžๆจ‚ๆคŽ้–“่žๅˆๅ™จ็ณป็ตฑ
Risk Class 2

Registration Details

5bc96fbdd9efd89bc5a0727cb234b260

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N.3080 ๆคŽ้ซ”้–“่žๅˆ่ฃ็ฝฎ

Domestic

Dates and Status

Mar 06, 2023

Mar 06, 2028